Lederer W J, Nelson M T
J Physiol. 1984 Mar;348:665-77. doi: 10.1113/jphysiol.1984.sp015132.
Ouabain-sensitive Na efflux, membrane potential and membrane current were measured in single, perfused muscle cells taken from the giant barnacle, Balanus nubilus. This preparation permits control of the intracellular and extracellular solution composition as well as control of the membrane potential while measuring ion fluxes across the plasma membrane. The addition of ouabain (10(-4) M) to the extracellular solution produces a rapid depolarization of membrane potential (1-4 mV) and a simultaneous and proportional reduction of Na efflux (10-40 pmol/s). Ouabain-induced changes in membrane potential or Na efflux do not depend on the presence of extracellular Na. Under voltage control, the application of ouabain (10(-4) M) produces a rapid monotonic fall in outward current (1-3 microA) and a simultaneous fall in Na efflux (10-40 pmol/s). The fraction of ouabain-dependent Na efflux that appears as outward current is constant in any given preparation as the Na-pump turnover rate varies. Over a limited range, changes in membrane potential do not affect ouabain-sensitive Na efflux. The ouabain-sensitive Na efflux and membrane current are not altered by the presence of 50 mM-internal tetraethylammonium (TEA) ions. We conclude that the Na pump is electrogenic in barnacle muscle and that 49 +/- 10% of the extruded Na+ leaves the intracellular compartment as uncompensated charge. We find that the transport stoicheiometry of Na:K, calculated from the ouabain-dependent changes in membrane current and Na efflux, is between 3:2 and slightly more than 2:1.
在取自巨型藤壶(Balanus nubilus)的单个灌注肌肉细胞中,测量了哇巴因敏感的钠外流、膜电位和膜电流。这种制备方法允许在测量跨质膜的离子通量时控制细胞内和细胞外溶液的组成以及膜电位。向细胞外溶液中添加哇巴因(10⁻⁴ M)会使膜电位迅速去极化(1 - 4 mV),同时钠外流会同步且成比例地减少(10 - 40 pmol/s)。哇巴因引起的膜电位或钠外流变化不依赖于细胞外钠的存在。在电压控制下,施加哇巴因(10⁻⁴ M)会使外向电流迅速单调下降(1 - 3 μA),同时钠外流也会下降(10 - 40 pmol/s)。在任何给定的制备中,随着钠泵周转率的变化,作为外向电流出现的哇巴因依赖性钠外流部分是恒定的。在有限范围内,膜电位的变化不会影响哇巴因敏感的钠外流。50 mM的细胞内四乙铵(TEA)离子的存在不会改变哇巴因敏感的钠外流和膜电流。我们得出结论,藤壶肌肉中的钠泵是生电的,并且挤出的Na⁺中有49 ± 10%作为未补偿电荷离开细胞内区室。我们发现,根据哇巴因依赖性的膜电流和钠外流变化计算得出的Na:K转运化学计量比在3:2到略大于2:1之间。